Hls5 regulated erythroid differentiation by modulating GATA-1 activity

Author:

Endersby Raelene12,Majewski Ian J.13,Winteringham Louise1,Beaumont Jennifer G.1,Samuels Amy1,Scaife Robin1,Lim Esther1,Crossley Merlin4,Klinken S. Peter1,Lalonde Jean-Philippe1

Affiliation:

1. Laboratory for Cancer Medicine, Western Australian Institute for Medical Research, Centre for Medical Research, University of Western Australia, Crawley, Australia;

2. Department of Developmental Neurobiology, St Jude Children's Research Hospital, Memphis, TN;

3. Division of Molecular Medicine, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia; and

4. School of Molecular and Microbial Biosciences, University of Sydney, Sydney, Australia

Abstract

Hemopoietic lineage switch (Hls) 5 and 7 were originally isolated as genes up-regulated during an erythroid-to-myeloid lineage switch. We have shown previously that Hls7/Mlf1 imposes a monoblastoid phenotype on erythroleukemic cells. Here we show that Hls5 impedes erythroid maturation by restricting proliferation and inhibiting hemoglobin synthesis; however, Hls5 does not influence the morphology of erythroid cells. Under the influence of GATA-1, Hls5 relocates from cytoplasmic granules to the nucleus where it associates with both FOG-1 and GATA-1. In the nucleus, Hls5 is able to suppress GATA-1–mediated transactivation and reduce GATA-1 binding to DNA. We conclude that Hls5 and Hls7/Mlf1 act cooperatively to induce biochemical and phenotypic changes associated with erythroid/myeloid lineage switching.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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